IVX-037 is under clinical development by ImmVirX and currently in Phase I for Adenocarcinoma Of The Gastroesophageal Junction. According to GlobalData, Phase I drugs for Adenocarcinoma Of The Gastroesophageal Junction have an 87% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IVX-037’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
IVX-037 overview
IVX-037 is under development for the treatment of unspecified cancer and solid tumors including metastatic colorectal cancer, gastric cancer, adenocarcinoma of the gastroesophageal junction, metastatic ovarian cancer and liver cancer. The therapeutic candidate comprises of oncolytic RNA viruses. It is administered through intratumoral and intravenous route.
ImmVirX overview
ImmVirX is developing a novel oncolytic immunotherapy that targets cancer indications. ImmVirX is headquartered in New Lambton Heights, New South Wales, Australia.
For a complete picture of IVX-037’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
